Characterisation of PM10 emissions from woodstove combustion of common woods grown in Portugal

A series of source tests was performed to evaluate the chemical composition of particle emissions from the woodstove combustion of four prevalent Portuguese species of woods: Pinus pinaster (maritime pine), Eucalyptus globulus (eucalyptus), Quercus suber (cork oak) and Acacia longifolia (golden wattle). Analyses included water-soluble ions, metals, radionuclides, organic and elemental carbon (OC and EC), humic-like substances (HULIS), cellulose and approximately l80 organic compounds. Particle (PM₁₀) emission factors from eucalyptus and oak were higher than those from pine and acacia. The carbonaceous matter represented 44–63% of the particulate mass emitted during the combustion process, regardless of species burned. The major organic components of smoke particles, for all the wood species studied, with the exception of the golden wattle (0.07–1.9% w/w), were anhydrosugars (0.2–17% w/w). Conflicting with what was expected, only small amounts of cellulose were found in wood smoke. As for HULIS, average particle mass concentrations ranged from 1.5% to 3.0%. The golden wattle wood smoke presented much higher concentrations of ions and metal species than the emissions from the other wood types. The results of the analysis of radionuclides revealed that the ²²⁶Ra was the naturally occurring radionuclide more enriched in PM₁₀. The chromatographically resolved organics included n-alkanes, n-alkenes, PAH, oxygenated PAH, n-alkanals, ketones, n-alkanols, terpenoids, triterpenoids, phenolic compounds, phytosterols, alcohols, n-alkanoic acids, n-di-acids, unsaturated acids and alkyl ester acids.     

Organic speciation of atmospheric particles in Alvão Natural Park (Portugal)

PM₁₀ continental rural background aerosols were collected during a summer field campaign (August–September 2006) at Lamas de Ôlo in the upper zone of the Alvão Natural Park, a mountain region of northern Portugal. In addition to the determination of the carbonaceous content by a thermal–optical method, the organic speciation of aerosols was performed by gas chromatography–mass spectrometry in an effort to evaluate photo-oxidation products of biogenic volatile organic compounds and other markers for source characterization. The detailed analysis revealed relatively high concentrations of polyols and short-chain dicarboxylic, tricarboxylic, hydroxycarboxylic, and oxocarboxylic acids, many of which are thought to be indicators of secondary aerosol formation, accounting for about 70% of global chromatographically resolved mass. Major photo-oxidation products of α- and β-pinene have been detected. The tracers for the photo-oxidation of isoprene comprise two diastereoisomeric 2-methyltetrols, C₅-alkene triols, and 2-methylglyceric acid, which have only recently been elucidated. In addition, the occurrence of levoglucosan and other biomass combustion tracers indicates that the site was affected by wildfires. This source contributed to more than 80% of the organic carbon mass during a period of strong forest fire influence.     

Löwenzahn Taraxacum officinale Web. als (städtischer) Bioindikator

Investigations of the dandelion, Taraxacum officinale Web. in Poland, Romania and Germany showed that the species concentrates various elements dependent on the intensity of the pollutants. In this study, we followed up the question of whether T. officinale enriches pollutants by the atmospheric deposition on the leaves or via the soil. Therefore, samples from at least 10 plants and a soil sample at 57 sample sites were collected from a grid of 500 m × 500 m. In addition to the analysis of the total soil sample, the (mobile) ion pool of the soil (DIN V 19739) was analysed. The elements Al, As, Ba, Ca, Cd, Ce, Co, Cr, Cu, Fe, Ga, K, Mg, Mn, Mo, Na, Ni, Rb, Sr, Ti, Tl, V, and Zn were determined through the use of spectrometry with inductive coupled plasma (ICP-MS and ICP-OES). The results are compared with the element concentrations of washed and unwashed leaf samples in T. officinale. We could only find two direct correlations (Ti and Zn) between the element content, of the entire soil samples, but 14 correlations (As, Ba, Cd, Cu, Ga, K, Mn, Mo, Na, Ni, Rb, Ti, Tl und Zn) between the ion pool of the soil and the washed samples. The grid point data interpolation by ArcInfo showed a similar distribution pattern for the unwashed leaf elements Al, Ce, Fe, Ti and V (r≥0.75). The elements Al, Ce, Fe, Ti, and V are washed out at the same ratio. Thus, although the concentration of these elements were significantly reduced by the washing procedure, the correlations were not influenced. The admissibility of the grid point data interpolation for a distribution map of the town area was investigated, as well. It is shown that the element content varies with the land use (meadow, field, rural areas), the sampling point and the local pollutants. However, none of the discussed elements, Al, Ce, Fe, Ti, and V, is significantly influenced by the land use. The data allows one to make the conclusion that the elements of Al, Ce, Fe, Ti and V are dependent on the dry and wet deposition on the leaves of T. officinale. These elements are taken up not only by the roots, but also by the surface of the leaves. This is evident because there is no correlation between one of these elements in the leaves and the ion pool of the soil.     

NitroGenius:氮决策支持系统--荷兰氮污染问题最佳解决方案的一个游戏模拟实验

利用计算机模拟的方法,我们为第二届国际氮会议研制开发了一个游戏形式的氮决策支持系统.研制这一系统的目的是:①使科学工作者和决策者们都能认识到荷兰氮污染问题的复杂性,因为荷兰是一个农业、工业和运输业活动密集的区域;②探索以最低的社会经济代价解决氮污染的最佳方案.NitroGenius由有关时空范围内的氮流动模型组成,其中包括氨和氮氧化合物的释放及其对地表水和地下水的污染.NitroGenius中还包括了一个经济模型,它描述了各个重要经济部门之间的关系,以及不同氮排放控制措施对国民生产总值(GDP)、失业率、能源消耗和环境的影响.在第二次国际氮会议期间,大约有50个研究组对NitroGenius进行了测试,结果表明,如果认真进行计划并选择适当的治理措施,就能够以适当的代价解决荷兰的氮污染问题.     

Agricultural soil as a potential source of input of organochlorine pesticides into a nearby pond

A study was conducted in the southeastern region of Buenos Aires province, Argentina, to assess an agricultural soil as a potential source of organochlorine (OC) pesticides for the aquatic biota of a nearby pond. We analyzed gamma-HCH (lindane), still in use, and the following banned compounds: DDT, DDE, DDD heptachlor, heptachlor epoxide, aldrin, dieldrin and endrin in soil, bulrush, grass shrimp and fish using gas chromatography with electron capture detection (GC-ECD). Among the OC pesticides, lindane was most dominant in the soil (32.6 ng/g dry wt in the upper and 173.9 ng/g dry wt in the lower horizon) and bulrush (1.9 pg/g lipid). Macrophyte also accumulated high levels of heptachlor epoxide (1.5 pg/g lipid). Heptachlor, although present in the soil, was below the detection limit in all aquatic biota studied. Its primary degradation product, heptachlor epoxide, was found in both soil and biota samples. DDT was found at low levels in the surface soil (6.8 ng/g dry wt), but at higher concentrations in fish (3.6 pg/g lipid), although levels were still below permissible levels for human consumption. Since most of the compounds were found in both soil and aquatic biota, our study suggests that agricultural soil could be an important source for OC pesticides in the nearby pond.     

Coefficient of variation of sea surface temperature (SST) as an indicator of coral bleaching

Coral bleaching has become a major problem on reefs around the world in recent decades. It is believed that mean temperature alone is the primary force driving this ecological phenomenon. We propose that variance in temperature in the short term is just as important as the mean. Thirty years of daily sea surface temperature (SST) data have been collected by the University of Puerto Rico at Mayaguez Marine Laboratory in La Parguera, PR. These data were collated and analyzed initially (by Amos Winter) for their relationship to coral bleaching in this area. We found that the data fell into three categories: high mean temperatures associated with severe bleaching, cooler mean temperatures associated with no bleaching, and years of high SSTs but with no coral bleaching. Here, we examined the relationship between mean temperature during those months in which bleaching occurred, temperature variance (as measured by standard deviation), and coefficient of variation (CV; i.e., SD standardized by the mean). We also derived a critical threshold temperature and level of resolution in time for calculating these statistics to clearly describe the circumstances of bleaching versus non-bleaching events, particularly at marginal bleaching temperatures. These characteristics were compared for the four warmest months of the year (July–October) for four warm bleaching years (1969, 1987, 1990, and 1995), four cool non-bleaching years (1984, 1985, 1986, and 1988), and two warm non-bleaching years (1994 and 2000). No relationship was found between the mean SST and SD in terms of predicting bleaching. The two primary statistics which, in concert, did indicate bleaching, however, were the short-term, biweekly mean temperature and its the associated CV. Bleaching occurs in association with both high temperatures and a high CV. The CV becomes a critical determinant of bleaching only when temperatures are ∼29.1–29.8°C. The warm, non-bleaching years were generally characterized by a CV of < 1.9 and a temperature range between 28.5 and 29.9°C. We conclude that increased mean SSTs alone are not sufficient to induce coral bleaching; a high variance in SST at marginal, lower bleaching temperatures can induce bleaching, and likewise, a low variance of such will not induce bleaching. This variance is most clearly described by the CV.     

Ingestion rate,assimilation efficiency and energy balance in Mytilus chilensis in relation to body size and different algal concentrations

Basing on a quantification of filtration, ingestion, assimilation, biodeposition, excretion and respiration rate, energy budgets were established in Mytilus chilensis Hupé in relation to body size and three different food concentrations of the unicellular green alga Dunaliella marina. The present quantifications revealed that in M. chilensis the ingestion rate only increases slightly with an increase in food concentration which, however, is counterbalanced by a significant decrease in assimilation efficiency in such a way that assimilation rate finally is nearly constant and independent of the food concentrations tested. The quantifications of these results are given by the a-values of the general allometric growth equation P=aW^b relating the energy disposable for growth and reproduction (P; cal d^-1 to body size (W; dry-tissue wt, g). The best energy budget was obtained at the lowest food concentration tested (0.8 mg algal dry wt l^-1; at 12°C and 30 S) with an a-value of 58.8, while the energy budget at the highest food concentration (2.14 mg l^-1) was only slightly lower with an a-value of 49.8; the b-values were 0.49 and 0.51, respectively. The net growth efficiencies (K₂) decreased with increasing body size (from 20 mg to 3 000 mg drytissue wt) from 76.7 to 47.9% at the lowest food level and from 72.6 to 44.0% at the highest food level tested. These relatively high net growth efficiencies seem to reflect optimal experimental conditions. Furthermore, by a comparison of estimated growth (calculated on the basis of the best energy budget) with growth actually quantified in culture raft mussels in the south of Chile during the highest production period of the year, it is obvious that the energy budgets established really reflect the conditions experienced by the mussels in their natural environment.This research was supported by grants S-80-3 and C-80-1 of the D.I.D.-UACH, by CONICYT, Found. Volkswagenwerk, Found. Fritz-Thyssen, by the GTZ, DFG and by the DAAD